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Method of producing aryl-substituted, amino-acylated phosphonic- acid derivatives with the aid of metal complexes of chiral, amphiphilic ligands

机译:借助手性两亲性配体的金属配合物生产芳基取代的氨基酰化的膦酸衍生物的方法

摘要

The invention is relates to a method of producing aryl- substituted, amino-acylated phosphonic-acid derivatives with the aid of metal complexes of chiral amphiphilic ligands in that according to the invention &agr;-N-acyl-protected, &bgr;-substituted alkene phosphone derivatives are asymmetrically hydrogenated in the presence of a chiral rhodium catalyst in a solvent or a suspension. The use of the micelle- forming catalyst makes possible the hydrogenation of unsaturated phosphonic-acid derivatives in water with a high reaction rate with the obtainment of very good enantiomeric excesses.
机译:本发明涉及借助于手性两亲性配体的金属配合物制备芳基取代的氨基酰化的膦酸衍生物的方法,其中根据本发明,α-N-酰基保护的,β-取代的烯烃在手性铑催化剂存在下,在溶剂或悬浮液中将膦衍生物进行不对称氢化。形成胶束的催化剂的使用使得能够以高反应速率在水中氢化不饱和膦酸衍生物,并且获得非常好的对映体过量。

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